Effect of water-soluble polymers on drug-cyclodextrin complexation

Chinese Pharmaceutical Journal

Volumn 34, Issue 2, 1999, Pages 99-101

  Wu, Wenjuan ^a   Chen, Yuzhen ^a   Tan, Zaiyou ^a  

^a GUANGDONG PHARMACEUTICAL UNIVERSITY   (China)

Author keywords

CD; Drugs; Inclusion association; Polymers

Indexed keywords

BETA CYCLODEXTRIN; CHLORAMPHENICOL; DRUG; MACROGOL; POLYMER; POVIDONE; RIBOFLAVIN; WATER;

AQUEOUS SOLUTION; ARTICLE; COMPLEX FORMATION; DRUG BINDING; DRUG SOLUBILITY; ENTHALPY; ENTROPY; SOLUBILIZATION; THERMODYNAMICS; VISCOSITY;

EID: 0032916319     PISSN: 10012494     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. Chinese source
2. Chinese source
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5. Higuchi T, Connors KA. Phase-solubility techniques. Adv Anal Instr.1965,4:117.
6. Brewster ME, Anderson WR, Loftsson T, et al. Preparation, characterization, and anesthetic properties of 2-hydroxypropyl-β-cyclodextrin complexes of pregnanolone and pregnenolone in rat and mouse. J Pharm Sci , 1995,84(10):1154.